Phosphate-driven H2O2 decomposition on DNA-bound bio-inspired activated carbon-based sensing platform for biological and food samples

被引:3
作者
Selvam, Sathish Panneer [1 ]
Cho, Sungbo [1 ,2 ]
机构
[1] Gachon Univ, Dept Elect Engn, Seongnam Si 13210, Gyeonggi Do, South Korea
[2] Gachon Univ, Gachon Adv Inst Hlth Sci & Technol, Incheon 21999, South Korea
基金
新加坡国家研究基金会;
关键词
Density functional theory; Salmon testes DNA; Self-assembly; Theobroma cacao; H2O2; HYDROGEN-PEROXIDE; HORSERADISH-PEROXIDASE; PERFORMANCE; ELECTRODE; SENSOR; CELLS; QUANTIFICATION; GRAPHENE; FILMS;
D O I
10.1016/j.foodchem.2023.136234
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Hydrogen peroxide (H2O2) is one of the most important reactive oxygen species (ROS). Increased endogenous H2O2 levels indicate oxidative stress and could be a potential marker of many diseases, including Alzheimer's, cardiovascular diseases, and diabetes. However, consuming H2O2-incorporated food has adverse effects on humans and is a serious health concern. We used salmon testes DNA with bio-inspired activated carbon (AC) as an electrocatalyst for developing a novel H2O2 sensor. The phosphate backbone of DNA contains negatively charged oxygen groups that specifically attract protons from H2O2 reduction. We observed a linearity range of 0.01-250.0 mu M in the H2O2 reduction peak current with a detection limit of 2.5 and 45.7 nM for chronoamperometric and differential pulse voltammetric studies. High biocompatibility of the sensor was achieved by the DNA, facilitating endogenous H2O2 detection. Moreover, this non-enzymatic sensor could also help in the rapid screening of H2O2-contaminated foods.
引用
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页数:13
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